礼来在PDA/FDA联合监管会议2026分享AI质量系统治理经验：连接GMP发现、审计与偏差

Karthik Iyer, Eli Lilly, detailed an AI system linking GMP findings, audits, and deviations for cited, inspection-ready regulatory intelligence.

At the PDA/FDA Joint Regulatory Conference 2026 in Washington, DC, Karthik Iyer, Associate Vice President, Compliance and Post Market Reporting, Eli Lilly, laid out a working model for how a global manufacturer is using AI to connect inspection findings, audit observations, and deviation data that traditionally live in separate systems.¹His presentation, "From Data Noise to Inspection Readiness: AI-Powered Regulatory Intelligence Across Your Quality Landscape," treated AI adoption less as a technology rollout and more as a governance exercise. Gourav Pandey, R&D Quality Lead, Takeda, and Svyatoslav Borshchenko, CEO and co-founder, GxPilot, covered this theme in an assessment of the FDA's April 2026 warning letter to Purolea Cosmetics Lab, which made clear that quality units, not algorithms, remain accountable for what AI-assisted systems produce. Taking a deeper dive into the topic here on pharmtech.com, Brian Drapeau, founder, GxPFrame, questioned whether compliant AI in pharma is even possible and explored how pharma’s next AI problem is authority.

What Questions Should a Quality Organization Ask Before Deploying AI?

Iyer claimed the most important questions were: Has a given signal occurred before, internally or externally? How does the enterprise share that signal without creating new exposure? What are the possible adverse inspection and possible litigation risks embedded in each data node? And how does a team guard against confirmation bias or sunk-cost thinking once a model starts producing answers it likes?¹ That final point lines up with concerns raised during the FDA's push toward digital-by-default oversight,² where connected, auditable records are treated as a prerequisite for AI use rather than a byproduct of it.

How Does the System Turn Documents into Defensible Answers?

Iyer walked through track findings by month, site, and health authority alongside Lilly's response and after-action review, with two AI layers sitting underneath it: a Document Explorer that applies retrieval-augmented generation to unstructured files such as inspection PDFs, and a Data Explorer for structured data sets.¹

What Did Lilly's Team Learn?

Iyer was candid about the tradeoffs.¹ Connecting the system to Lilly's data lake meant wrestling with translation issues, global stop-words, and parameter tuning to balance document volume against accuracy. He urged discipline in weighing outside expertise against internal judgment, and cautioned against using the tools to generate predictions or restate what a reviewer already knows, keeping the focus instead on surfacing a defensible range of outcomes.

Why the Emphasis on Hallucination Research?

Iyer cited the AA-Omniscience benchmark, which found hallucination rates ranging from 22% to 94% across 26 leading models, and noted a sharper finding: accuracy on identical false claims collapsed once a statement was framed as the user's own belief rather than a third party's, with GPT-4 falling from 98.2% to 64.4% and DeepSeek R1 from over 90% to 14.4%. He also pointed to a growing body of research showing that even long-context models lose accuracy as inputs grow. For a compliance function built on getting the source citation right, that's less a footnote than the whole point.

References

Parenteral Drug Association. PDA/FDA Join Regulatory Confernce 2026 Agenda. Available at https://www.pda.org/global-event-calendar/event-detail/pda-fda-joint-regulatory-conference-2026#agenda. Accessed Sept 15, 2026.
From guidance to operating model: preparing CMC and quality systems for FDA’s digital-by-default oversight. Pharmaceutical Technology. Accessed September 18, 2026. https://www.pharmtech.com/view/from-guidance-to-operating-model-preparing-cmc-quality-systems-for-fda-s-digital-by-default-oversight